ENST00000264381.8:c.1803T>G
MANE Select
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ENSP00000264381.3:p.Gly601=
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ENST00000264381.7:c.1803T>G
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ENSP00000264381.3:p.Gly601=
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ENST00000479451.5:c.393T>G
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ENSP00000418325.1:p.Gly131=
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ENST00000482958.1:c.*309T>G
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ENSP00000419804.1:n.*309T>G
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ENST00000497011.5:c.*193T>G
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ENSP00000419505.1:n.*193T>G
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NM_000055.2:c.1803T>G
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NP_000046.1:p.Gly601=
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XM_005247685.1:c.1926T>G
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XP_005247742.1:p.Gly642=
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NM_000055.3:c.1803T>G
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NP_000046.1:p.Gly601=
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NR_137635.1:n.445T>G
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NR_137636.1:n.2049T>G
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NM_000055.4:c.1803T>G
MANE Select
|
NP_000046.1:p.Gly601=
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NR_137635.2:n.396T>G
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|
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NR_137636.2:n.2000T>G
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